Climatic changes and their role in emergence and re-emergence of diseases
Identifieur interne : 000146 ( Pmc/Corpus ); précédent : 000145; suivant : 000147Climatic changes and their role in emergence and re-emergence of diseases
Auteurs : Amr El-Sayed ; Mohamed KamelSource :
- Environmental Science and Pollution Research International [ 0944-1344 ] ; 2020.
Abstract
Global warming and the associated climate changes are predictable. They are enhanced by burning of fossil fuels and the emission of huge amounts of CO2 gas which resulted in greenhouse effect. It is expected that the average global temperature will increase with 2–5 °C in the next decades. As a result, the earth will exhibit marked climatic changes characterized by extremer weather events in the coming decades, such as the increase in temperature, rainfall, summertime, droughts, more frequent and stronger tornadoes and hurricanes. Epidemiological disease cycle includes host, pathogen and in certain cases intermediate host/vector. A complex mixture of various environmental conditions (e.g. temperature and humidity) determines the suitable habitat/ecological niche for every vector host. The availability of suitable vectors is a precondition for the emergence of vector-borne pathogens. Climate changes and global warming will have catastrophic effects on human, animal and environmental ecosystems. Pathogens, especially neglected tropical disease agents, are expected to emerge and re-emerge in several countries including Europe and North America. The lives of millions of people especially in developing countries will be at risk in direct and indirect ways. In the present review, the role of climate changes in the spread of infectious agents and their vectors is discussed. Examples of the major emerging viral, bacterial and parasitic diseases are also summarized.
Url:
DOI: 10.1007/s11356-020-08896-w
PubMed: NONE
PubMed Central: 7187803
Links to Exploration step
PMC:7187803Le document en format XML
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<front><div type="abstract" xml:lang="en"><p id="Par1">Global warming and the associated climate changes are predictable. They are enhanced by burning of fossil fuels and the emission of huge amounts of CO<sub>2</sub>
gas which resulted in greenhouse effect. It is expected that the average global temperature will increase with 2–5 °C in the next decades. As a result, the earth will exhibit marked climatic changes characterized by extremer weather events in the coming decades, such as the increase in temperature, rainfall, summertime, droughts, more frequent and stronger tornadoes and hurricanes. Epidemiological disease cycle includes host, pathogen and in certain cases intermediate host/vector. A complex mixture of various environmental conditions (e.g. temperature and humidity) determines the suitable habitat/ecological niche for every vector host. The availability of suitable vectors is a precondition for the emergence of vector-borne pathogens. Climate changes and global warming will have catastrophic effects on human, animal and environmental ecosystems. Pathogens, especially neglected tropical disease agents, are expected to emerge and re-emerge in several countries including Europe and North America. The lives of millions of people especially in developing countries will be at risk in direct and indirect ways. In the present review, the role of climate changes in the spread of infectious agents and their vectors is discussed. Examples of the major emerging viral, bacterial and parasitic diseases are also summarized.</p>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Environ Sci Pollut Res Int</journal-id>
<journal-id journal-id-type="iso-abbrev">Environ Sci Pollut Res Int</journal-id>
<journal-title-group><journal-title>Environmental Science and Pollution Research International</journal-title>
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<issn pub-type="ppub">0944-1344</issn>
<issn pub-type="epub">1614-7499</issn>
<publisher><publisher-name>Springer Berlin Heidelberg</publisher-name>
<publisher-loc>Berlin/Heidelberg</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmc">7187803</article-id>
<article-id pub-id-type="publisher-id">8896</article-id>
<article-id pub-id-type="doi">10.1007/s11356-020-08896-w</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Review Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Climatic changes and their role in emergence and re-emergence of diseases</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>El-Sayed</surname>
<given-names>Amr</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author" corresp="yes"><name><surname>Kamel</surname>
<given-names>Mohamed</given-names>
</name>
<address><email>m_salah@staff.cu.edu.eg</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<aff id="Aff1"><institution-wrap><institution-id institution-id-type="GRID">grid.7776.1</institution-id>
<institution-id institution-id-type="ISNI">0000 0004 0639 9286</institution-id>
<institution>Department of Medicine and Infectious Diseases, Faculty of Veterinary Medicine,</institution>
<institution>Cairo University,</institution>
</institution-wrap>
Giza, Egypt</aff>
</contrib-group>
<author-notes><fn fn-type="com"><p>Responsible editor: Lotfi Aleya</p>
</fn>
</author-notes>
<pub-date pub-type="epub"><day>28</day>
<month>4</month>
<year>2020</year>
</pub-date>
<fpage>1</fpage>
<lpage>17</lpage>
<history><date date-type="received"><day>26</day>
<month>2</month>
<year>2020</year>
</date>
<date date-type="accepted"><day>14</day>
<month>4</month>
<year>2020</year>
</date>
</history>
<permissions><copyright-statement>© Springer-Verlag GmbH Germany, part of Springer Nature 2020</copyright-statement>
<license><license-p>This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p>
</license>
</permissions>
<abstract id="Abs1"><p id="Par1">Global warming and the associated climate changes are predictable. They are enhanced by burning of fossil fuels and the emission of huge amounts of CO<sub>2</sub>
gas which resulted in greenhouse effect. It is expected that the average global temperature will increase with 2–5 °C in the next decades. As a result, the earth will exhibit marked climatic changes characterized by extremer weather events in the coming decades, such as the increase in temperature, rainfall, summertime, droughts, more frequent and stronger tornadoes and hurricanes. Epidemiological disease cycle includes host, pathogen and in certain cases intermediate host/vector. A complex mixture of various environmental conditions (e.g. temperature and humidity) determines the suitable habitat/ecological niche for every vector host. The availability of suitable vectors is a precondition for the emergence of vector-borne pathogens. Climate changes and global warming will have catastrophic effects on human, animal and environmental ecosystems. Pathogens, especially neglected tropical disease agents, are expected to emerge and re-emerge in several countries including Europe and North America. The lives of millions of people especially in developing countries will be at risk in direct and indirect ways. In the present review, the role of climate changes in the spread of infectious agents and their vectors is discussed. Examples of the major emerging viral, bacterial and parasitic diseases are also summarized.</p>
</abstract>
<kwd-group xml:lang="en"><title>Keywords</title>
<kwd>Climate</kwd>
<kwd>Climate change</kwd>
<kwd>Global warming</kwd>
<kwd>Disease</kwd>
<kwd>Vector</kwd>
<kwd>Mosquitoes</kwd>
<kwd>Tick</kwd>
<kwd>Sandflies</kwd>
<kwd>West Nile</kwd>
<kwd>Lyme</kwd>
<kwd>Malaria</kwd>
<kwd>Zika</kwd>
<kwd>Ticks</kwd>
<kwd>Tick-borne diseases</kwd>
<kwd>Emerging and resurging pathogens</kwd>
<kwd>Zoonoses</kwd>
<kwd>Vector ecology</kwd>
</kwd-group>
</article-meta>
</front>
<body><sec id="Sec1"><title>Introduction</title>
<p id="Par2">According to the World Health Organization (WHO), the “climate change and global warming” are the greatest challenges of humanity in the twenty-first century. They threaten all aspects of our life (Organization WH <xref ref-type="bibr" rid="CR139">2018</xref>
). Climate change and global warming are two expressions which are usually used in an interchangeable manner although global warming is just one aspect of various aspects associated with climate change. The expression “global warming” usually refers to the observed rise in average global temperature in the last decades in terms of frequency and intensity. It is induced by the greenhouse effect due to the increase in CO<sub>2</sub>
emissions produced by the increasing consumption of fossil fuels worldwide in parallel with cutting trees/forests. The rise in temperature increases toward the poles and is less near the equator. It accelerates with time and is expected to be faster in the next years and may range between + 1.6 and + 6 °C according to the computer simulator scenarios (IPC C <xref ref-type="bibr" rid="CR84">2001</xref>
; IPPC <xref ref-type="bibr" rid="CR85">2017</xref>
; Jimenez-Clavero <xref ref-type="bibr" rid="CR89">2012</xref>
; Solomon et al. <xref ref-type="bibr" rid="CR175">2007</xref>
). The global warming-related changes in disease epidemiology are associated with changes in ecosystems, population susceptibility and increased exposure to causative agents (Ghazali et al. <xref ref-type="bibr" rid="CR65">2018</xref>
). Global warming also affects the geographical distribution of vectors/intermediate host distribution, including invertebrate hosts (insects), rodents and migratory birds. As an example, the zoonotic bacteria pathogen (Chlamydia) can be carried by birds and infects 92 million people annually according to the WHO. The zoonotic bacteria pathogen can be carried by birds and infects 92 million people annually according to the WHO. The disease is associated with bird movement and migration which is, in turn, influenced by the climatic and ecological changes (Geisler <xref ref-type="bibr" rid="CR64">2012</xref>
) On the other hand, the term “climate change” refers to observed measurable changes of the climate over a long period of time. Climatic changes are characterized by extremer weather events, accompanied by the increase in the prevalence of droughts, heat waves, extreme rainfalls and floods or dryness and water scanty, dust storms, tropical cyclones (typhoons or hurricanes), wildfires, melting of snow and disappearance of river delta and coastal cities in addition to environmental changes such as habitat fragmentation, bushmeat consumption, urbanization and deforestation (Handmer et al. <xref ref-type="bibr" rid="CR75">2012</xref>
; Nava et al. <xref ref-type="bibr" rid="CR131">2017</xref>
). The negative effects of global warming and climatic changes on human health are largely underestimated. It is estimated that 34% of all childhood illness and 36% of young children’s deaths worldwide are linked to changes in the environmental factors. Outbreaks of cholera, fatal malaria, diarrhoea or dengue fever are all strongly influenced by climatic changes (Thompson et al. <xref ref-type="bibr" rid="CR184">2012</xref>
).</p>
<p id="Par3">Climatic changes can result in change of human socio-demographics (Fig. <xref rid="Fig1" ref-type="fig">1</xref>
) and massive migration of humans and domestic livestock from dry hot areas to new geographic districts where the life circumstances are better (El-Sayed and Awad <xref ref-type="bibr" rid="CR52">2018</xref>
). This is accompanied with changes in the classical geographical distribution of wild animals, insects, rodents, and their population worldwide (Mor et al. <xref ref-type="bibr" rid="CR128">2018</xref>
). The interaction and the epidemiological relationship between climatic changes, environmental and ecosystem disturbance, exposure to vector insects and spread of infectious disease is well documented (Greer et al. <xref ref-type="bibr" rid="CR70">2008</xref>
; Organization WH <xref ref-type="bibr" rid="CR138">2005</xref>
; Teklehaimanot et al. <xref ref-type="bibr" rid="CR182">2004</xref>
). Understanding this link enables the prediction of the expected effects of climatic changes in the near future on the ecology of infectious agents, the spread of pathogens, vectors (intermediate hosts), reservoir animals, and final hosts (Medone et al. <xref ref-type="bibr" rid="CR118">2015</xref>
).<fig id="Fig1"><label>Fig. 1</label>
<caption><p>Effect of climatic changes on emerging of infectious diseases</p>
</caption>
<graphic xlink:href="11356_2020_8896_Fig1_HTML" id="MO1"></graphic>
</fig>
</p>
<p id="Par4">One of the absolutely underestimated threats of global warming is the melting of ice layer existing since thousands of years. Melting ice will not only lead to the disappearance of many cities and river delta but will also reactivate frozen biological materials stored in frozen soil. Melting of ice layer will not only provide us with buried carcasses of animals since thousands of years like mammoth, but unfortunately, additional hidden biological materials are also buried under snow. In 2012, Virola virus was detected in a 300 old frozen mummy in Siberian (Biagini et al. <xref ref-type="bibr" rid="CR20">2012</xref>
). While scientists from NASA in 2005 could revive bacteria stored frozen in Alaska since 32,000 years, others could isolate 8-million-year-old bacteria from ice samples in Antarctica (Bidle et al. <xref ref-type="bibr" rid="CR21">2007</xref>
). Viable bacteria could also be isolated from ice sample 25,000 years old (Katayama et al. <xref ref-type="bibr" rid="CR92">2007</xref>
) and from Dominican amber (20–40 million years old) (Greenblatt et al. <xref ref-type="bibr" rid="CR69">1999</xref>
). In 2016 in Siberian, a 12-year-old child died and 20 persons were hospitalized due to anthrax infections. The spores were hidden over 75 under frozen soil before being liberated as the ice melt. Anthrax is caused by <italic>Bacillus anthracis</italic>
, a spore-forming bacterium. The spores are very resistant in the environment and can survive/persist for a hundred years in a dormant form. The spores can be transported by floods or by insects (e.g. tabanid flies). Following the same concept, it is imaginable that smallpox virus could also be stored frozen in frozen human bodies buried in frozen soil in Siberian where a large epidemic of small pox occurred in 1890 (Antonenko et al. <xref ref-type="bibr" rid="CR7">2013</xref>
; Mor et al. <xref ref-type="bibr" rid="CR128">2018</xref>
).</p>
<p id="Par5">The WHO listed the health hazards on human health due to climatic changes into the following item (Fig. <xref rid="Fig2" ref-type="fig">2</xref>
): (1) direct and indirect effects of global warming, (2) stratospheric ozone depletion, (3) disturbance in terrestrial and marine ecosystems, (4) loss of biodiversity, (5) changes in the hydrological systems and freshwater supply, (6) Land degradation and loss of river deltas and coastal cities, (7) urbanization, deforestation and population dislocation/immigration, and finally (8) limited food production (WHO <xref ref-type="bibr" rid="CR194">2017</xref>
). These direct and indirect effects of the climatic shift on human/animal health and welfare include: (1). The direct influences result from physio-psychological effects from the increased number and duration of heat waves leading to stress, respiratory, circulatory collapse, heat strokes, and the long-term effects include squamous-cell carcinoma. The direct effects also include the negative effects of floods, droughts and storms on the wildlife and forests. The global warming directly influences the abundance, survival, and distribution of pathogens and their vectors. Meanwhile, (2) the indirect effects include famines and the negative effects of massive migratory waves of human/animal populations (Smith et al. <xref ref-type="bibr" rid="CR174">2017</xref>
) and the resulting ecological shift is predicted—using an optimistic scenario—to induce at least 250,000 additional deaths annually between 2030 and 2050. Out of these, 48,000 are expected to die due to diarrhoea, 60,000 due to malaria and the rest due to malnutrition and heat strokes. Unfortunately, the poor developing countries are the most vulnerable countries although they are the least responsible for the CO<sub>2</sub>
emission and greenhouse effect (Dhimal et al. <xref ref-type="bibr" rid="CR45">2015a</xref>
). It is alarming to know that more than 60% of human infectious diseases which emerged between 1940 and 2004 were zoonotic diseases of animal origin. This has a great impact on public health and world economy. Out of these, 22.8% are arthropod-borne diseases, and 71.8% originated from wildlife (Dantas-Torres <xref ref-type="bibr" rid="CR40">2015</xref>
). It was unexpected that Nepal became endemic for many major vector-borne diseases (VBDs), although the land lies at high altitude due to Himalaya mountains. The diseases include malaria, leishmaniasis, filariasis, Japanese encephalitis and dengue fever (Dhimal et al. <xref ref-type="bibr" rid="CR45">2015a</xref>
).<fig id="Fig2"><label>Fig. 2</label>
<caption><p>Health hazard on human health due to climatic changes</p>
</caption>
<graphic xlink:href="11356_2020_8896_Fig2_HTML" id="MO2"></graphic>
</fig>
</p>
<p id="Par6">Emerging infectious diseases (EIDs) could be defined as infectious diseases which increase (their prevalence or threaten) over time. They include (1) new unknown diseases which are first diagnosed and (2) old diseases which evolved or mutated from already existing agents and gained new features (i.e. adaptation to new hosts or target population, new geographic distribution, new clinical picture, new epidemiological profile, new spread pattern or resistance to used therapeutics). The events that drive emerging of infectious diseases were illustrated in Fig. <xref rid="Fig3" ref-type="fig">3</xref>
. Endemic diseases may also re-emerge where they are endemic (i.e. release epidemics or their prevalence increases clearly). Meanwhile, the re-emerging diseases could be defined as new infections resulting from unknown or newly introduced pathogen to a new geographic area (Dikid et al. <xref ref-type="bibr" rid="CR47">2013</xref>
; Epizooties OId <xref ref-type="bibr" rid="CR54">2014</xref>
; Ogden and Gachon <xref ref-type="bibr" rid="CR135">2019</xref>
). The major emerging and re-emerging infectious agents in the last decade included Ebola virus (Africa), Middle East respiratory syndrome coronavirus (Middle East) and Zika, chikungunya, yellow fever and dengue viruses (North and South America) (Ogden and Gachon <xref ref-type="bibr" rid="CR135">2019</xref>
). The CDC listed at least 50 emerging/re-emerging diseases worldwide. Some common examples of emerging and re-emerging diseases infecting human, animals or both were listed in Table <xref rid="Tab1" ref-type="table">1</xref>
. The list included Bovine spongiform encephalopathy, campylobacteriosis, Chagas disease, cholera, <italic>Cryptococcus</italic>
, cryptosporidiosis, cyclosporiasis, cysticercosis, dengue fever, diphtheria, drug-resistant infections (antimicrobial resistance), Ebola haemorrhagic fever, <italic>Escherichia coli</italic>
infection, group B streptococcus, hantavirus pulmonary syndrome, Hendra virus, hepatitis C, histoplasmosis, HIV/AIDS, influenza, Lassa fever, Legionnaires’ disease, leptospirosis, listeriosis, Lyme disease, malaria, Marburg haemorrhagic fever, measles, monkeypox, MRSA, Nipah virus, norovirus, pertussis, plague, poliomyelitis, rabies, Rift Valley fever, rotavirus, salmonellosis, severe acute respiratory syndrome, shigellosis, sleeping sickness (trypanosomiasis), smallpox, tuberculosis, tularemia, valley fever (coccidioidomycosis), vancomycin-intermediate or vancomycin-resistant, <italic>Staphylococcus aureus</italic>
, West Nile virus and yellow fever which are mainly insect-borne, airborne, water-borne and foodborne diseases (Smith et al. <xref ref-type="bibr" rid="CR174">2017</xref>
). The published disease list includes mainly of the so-called neglected tropical diseases (NTDs). NTDs are a group of bacterial, viral, parasitic and fungal pathogens usually endemic in tropical and subtropical developing countries. As these diseases are usually limited to poor countries, the pharma industry did not invest enough money to solve these problems until they started to expand and represent a real threat to the developed world. According to WHO, 20 core NTDs are candidates to re-emerge in the developed countries due to global warming namely; the dengue fever and rabies (viral diseases), buruli ulcer (<italic>Mycobacterium ulcerans</italic>
infection), trachoma (<italic>Chlamydia trachomatis</italic>
), yaws (spirochete), treponematoses, and leprosy (bacterial diseases), Chagas disease, trypanosomiasis, leishmaniasis, dracunculiasis, cysticercosis, echinococcosis, foodborne trematodiases, lymphatic filariasis, onchocerciasis (river blindness), schistosomiasis, and soil-transmitted helminthiases (ascariasis, hookworm, trichuriasis) (parasitic diseases) (El-Sayed and Awad <xref ref-type="bibr" rid="CR52">2018</xref>
; Mackey et al. <xref ref-type="bibr" rid="CR109">2014</xref>
; Mitra and Mawson <xref ref-type="bibr" rid="CR123">2017</xref>
). These neglected tropical pathogens may re-emerge again due to the expansion of the vector hosts (insect/rodent-borne diseases), by wind (airborne diseases), floods (water-borne diseases), migration of human/domestic or wild populations, even melting the accumulated snow due to the global warming may liberate the (sleeping) spores (e.g. anthrax). Importation of exotic pets may also play a role in the introduction of new pathogens or parasites to free locations (Andreassen et al. <xref ref-type="bibr" rid="CR6">2012</xref>
, Dhimal et al. <xref ref-type="bibr" rid="CR45">2015a</xref>
, Mackey et al. <xref ref-type="bibr" rid="CR109">2014</xref>
, Mitra &Mawson 2017). However, it was observed that the effect of the climatic changes on the vectors is not equal. For instance, the geographical expansion of mosquitoes is affected not only by the increase in temperature but also by the wind intensity and direction, relative humidity and rainfalls in opposite to ticks. This is attributed to the life cycle of mosquitoes which depend on one stagnant water for laying eggs and for the development of larval stages. Reports concerning the increase in the prevalence of malaria due to climatic changes are already published in Iran (Babaie et al. <xref ref-type="bibr" rid="CR11">2018</xref>
) and Zimbabwe (Gunda et al. <xref ref-type="bibr" rid="CR71">2017</xref>
).<fig id="Fig3"><label>Fig. 3</label>
<caption><p>Events triggering the emergence of infectious diseases</p>
</caption>
<graphic xlink:href="11356_2020_8896_Fig3_HTML" id="MO3"></graphic>
</fig>
<table-wrap id="Tab1"><label>Table 1</label>
<caption><p>Influence of climatic changes on health and diseases</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th colspan="12">How climatic changes influence health and diseases:</th>
</tr>
<tr><th rowspan="2" colspan="2">Agriculture (food)</th>
<th rowspan="2" colspan="2">Water resources</th>
<th rowspan="2">Tornados and wind</th>
<th colspan="5">Increase temperature and humidity</th>
<th rowspan="2" colspan="2">Mass migration of</th>
</tr>
<tr><th colspan="2">Expansion of insect niche</th>
<th colspan="2">Rodent niche</th>
<th>Direct effects on Human health</th>
</tr>
<tr><th>Food scanty</th>
<th>Foodborne diseases</th>
<th>Water scanty</th>
<th>Rains and floods</th>
<th>Airborne diseases</th>
<th>Insect/parasites</th>
<th>Insect-borne diseases</th>
<th>Rodents</th>
<th>Rodent-borne diseases</th>
<th>Physical and psychological diseases</th>
<th>Human</th>
<th>Animals</th>
</tr>
</thead>
<tbody><tr><td><p>- Diseases caused by consumption of rotted food</p>
<p>- Nutritional deficiency diseases</p>
</td>
<td><p>- Bacteria (e.g. Salmonellosis)</p>
<p>- Viral (e.g. Hepatitis A)</p>
</td>
<td><p>-Diseases due to consumption of contaminated water (e.g. cholera, hepatitis A, giardiasis and cryptosporidiosis)</p>
<p>-Dehydration and famines</p>
</td>
<td><p>- Fungal diseases and mycotoxins</p>
<p>- Water-borne diseases</p>
<p>- Spore-borne diseases (washed away via floods e.g. Anthrax).</p>
<p>- Snail-borne diseases (e.g. trematodes)</p>
</td>
<td>-In human (e.g. wind pox) and animals (e.g. FMD).</td>
<td><p>- Such as mosquitoes</p>
<p>Ticks</p>
<p>Flies</p>
<p>Flea</p>
</td>
<td><p>- Including bacterial, viral and parasitic diseases as West Nile fever</p>
<p>Plague</p>
<p>Malaria and leishmaniasis</p>
</td>
<td>- The spread of rats and mice which has health and economic impacts</td>
<td><p>- Hanta disease</p>
<p>-Leptospirosis</p>
</td>
<td><p>- Physical diseases (e.g. sun struck, respirator asthma and heart diseases)</p>
<p>- Psychological diseases and stress-borne diseases</p>
</td>
<td>Because of wars and famines which spread diseases in addition to its economic impacts</td>
<td>Due to water and food scanty which spread diseases to new areas</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
<p id="Par7">The invasion of new parasites and their emergence to free areas is also seen in the aquatic ecosystem. In Canada, parasitological investigations of the Laurentian Great Lakes basin determined at least 182 non-indigenous invading parasite species, i.e. a new invader species emerges every 28 weeks (Marcogliese <xref ref-type="bibr" rid="CR113">2008</xref>
; Ricciardi <xref ref-type="bibr" rid="CR164">2006</xref>
). The increase in seawater temperature-induced severe diseases to corals reefs which started to die. Coral reefs represent safe housing and food for several fish types. The increase in water temperature also leads to a decrease in the amounts of dissolved oxygen in the water. All these factors lead to great disturbance in the aqua ecosystem (Hakalahti et al. <xref ref-type="bibr" rid="CR73">2006</xref>
; Harvell et al. <xref ref-type="bibr" rid="CR79">1999</xref>
; Hayes et al. <xref ref-type="bibr" rid="CR80">2001</xref>
).</p>
</sec>
<sec id="Sec2"><title>NTDs</title>
<p id="Par8">In the last years, the flow of refugees and illegal immigrants seeking asylum, coming from war/famine suffering countries increased the prevalence of many of the NTDs or their re-emergence in western countries. One of the best examples is the human scabies caused by Sarcoptes scabiei mites. Although the parasitic disease has a global distribution, the prevalence in Europe was very low (Chandler and Fuller <xref ref-type="bibr" rid="CR34">2019</xref>
). Outbreaks of scabies in Europe could be observed in the last decade such as in Kindergarten in Germany in 2013 (Ariza et al. <xref ref-type="bibr" rid="CR9">2013</xref>
) and in German Health Care Centre (Leistner et al. <xref ref-type="bibr" rid="CR103">2017</xref>
) and in elderly home in the UK (Cassell et al. <xref ref-type="bibr" rid="CR30">2018</xref>
). Other parasitic diseases are also involved in the NTD list, such as the following: (1) dracunculiosis (or guinea worm disease), dracunculiasis a parasitic water-borne disease caused by <italic>Dracunculus medinensis</italic>
and occurs following drinking contaminated water (Biswas et al. <xref ref-type="bibr" rid="CR22">2013</xref>
); (2) lymphatic filariasis (elephantiasis), a parasitic disease which obstructs the lymph vessels of the lower extremities and is transmitted by a wide range of mosquitoes, but the main vector is <italic>Anopheles</italic>
and <italic>Culex quinquefasciatus</italic>
(Control CfD, Prevention <xref ref-type="bibr" rid="CR36">2013</xref>
); (3) onchocerciasis (or river blindness), a parasitic disease caused by the nematode <italic>Onchocerca volvulus</italic>
and transmitted by blackflies (CDC <xref ref-type="bibr" rid="CR32">2017b</xref>
); and (4) internal parasites including GIT nematodes and other trematodes such as <italic>Fasciola</italic>
spp. and <italic>Schistosoma</italic>
spp. They are very sensitive for climatic conditions which control their expansion pattern. For instance, floods, rainfalls, and the increased climatic temperature and humidity enable the survival of the free-living stages of the parasites (larva/metacercaria) and therefore increases disease prevalence. Schistosomiasis, Swimmer’s itch or bilharzia are five species of trematodes belonging to the genus <italic>Schistosoma</italic>
which require snails as intermediate hosts. The flocks invade the body through the skin (Mas-Coma et al. <xref ref-type="bibr" rid="CR114">2008</xref>
) (CDC <xref ref-type="bibr" rid="CR31">2017a</xref>
). The global warming expanded the habitat of the snail to a new land so that the disease is increasingly recorded in Europe (De Gentile et al. <xref ref-type="bibr" rid="CR41">1996</xref>
; Kolarova <xref ref-type="bibr" rid="CR98">2007</xref>
; Larsen et al. <xref ref-type="bibr" rid="CR102">2004</xref>
). Recently, in 2015, an outbreak of urogenital schistosomiasis occurred in France. The victims were from France, Germany and Italy (Boissier et al. <xref ref-type="bibr" rid="CR24">2015</xref>
). The snail vector of Schistosoma was also recorded in East Europe (Majoros et al. <xref ref-type="bibr" rid="CR110">2008</xref>
; Pointier et al. <xref ref-type="bibr" rid="CR151">2005</xref>
). Other snail mediated trematode parasites such as <italic>Fasciola</italic>
, <italic>Clonorchis</italic>
, <italic>Opisthorchis</italic>
and <italic>Paragonimus</italic>
also expand in a similar manner in association with the expansion of host to new geographical locations (Morgan et al. <xref ref-type="bibr" rid="CR129">2001</xref>
). <italic>Fasciola hepatica</italic>
is a zoonotic re-emerging neglected tropical parasite which infects mainly grazing sheep and cattle. The global warming increases the survival and expansion of the free-living cercaria and snail vector and at the same time, the increase of grazing season increases the exposure of the grazing animals to the parasite. Therefore and as expected, the prevalence of Fascioliasis increased in the last decade in endemic countries (Beesley et al. <xref ref-type="bibr" rid="CR15">2018</xref>
).</p>
<p id="Par9">Beside the previously mentioned parasitic diseases, NTDs of viral origin are also involved in the list, among them are as follows: (1) rabies, which is one of the most serious re-emerging zoonotic NTDs—the free movement of wild animals represents a great obstacle in disease control (El-Sayed <xref ref-type="bibr" rid="CR51">2018</xref>
; Hampson et al. <xref ref-type="bibr" rid="CR74">2015</xref>
); (2) dengue fever, a serious viral disease which has four serotypes. The disease is transmitted by mosquitoes mainly <italic>Aedes aegypti</italic>
and <italic>Ae</italic>
. <italic>albopictus</italic>
and is responsible for 96 million new infections yearly worldwide annual cases. Out of these, only 500,000 patients develop severe symptoms and 1250 fatalities (Dhar-Chowdhury et al. <xref ref-type="bibr" rid="CR44">2017</xref>
). (3) Ebola haemorrhagic fever and the closely related Marburg fever. Both are fatal zoonotic viral diseases virus. Epidemiological studies linked outbreaks with climatic changes specially the rainfall/dryness seasonal patterns. Therefore, it is expected that global warming will affect the geographical distribution of both diseases (Schmidt et al. <xref ref-type="bibr" rid="CR170">2017</xref>
).</p>
<p id="Par10">Possibly one of the most serious emerging NTDs of bacterial origin is the leprosy. The disease is caused by <italic>mycobacterium lepra</italic>
. Although leprosy was eradicated from Europe since hundreds of years, the NTDs emerged partially in some European countries recently. In Spain, between 2003 and 2013, a sum of 168 leprosy cases was registered. Out of them, 40 people were Spanish patients, while the remaining were illegal immigrants (Ramos et al. <xref ref-type="bibr" rid="CR157">2016</xref>
).</p>
</sec>
<sec id="Sec3"><title>Foodborne and water-borne diseases</title>
<p id="Par11">Water-borne and foodborne diseases are a serious public health concern worldwide. Water-borne and foodborne outbreaks are closely associated with climatic changes and disturbances in the ecosystem. They are more common in the summertime and increase with rising temperatures and humidity (Greer et al. <xref ref-type="bibr" rid="CR70">2008</xref>
). In addition, among the expected climate changes is the increase in frequencies of floods and heavy rainfalls due to warming of the oceans and due to the increase in frequency and strength of Al Nino and Hurricanes. This, in turn, will be reflected on the increase in water-borne diseases as giardiasis, cryptosporidiosis, infections with pathogenic <italic>E. coli</italic>
, <italic>Shigella</italic>
, cholera, <italic>Salmonella</italic>
, and viral hepatitis A (Haines and Patz <xref ref-type="bibr" rid="CR72">2004</xref>
). Consequently, floods and the increase in water volume will lead to the overload of sewage drainage systems and their overflow and contamination of drinking water. The increase in global temperature will also enhance the emergence of freshwater snails to free areas which enable the expansion of snail mediated trematodes (McCarthy et al. <xref ref-type="bibr" rid="CR115">2001</xref>
; Portier et al. <xref ref-type="bibr" rid="CR153">2017</xref>
). Therefore, global warming will result in a significant and serious increase in the worldwide prevalence of enteric/diarrhoeal diseases, but it can even induce fatal epidemics such as epidemics caused by fatal thermophilic free-living amoeba the <italic>Naegleria fowleri</italic>
which induce fatal meningoencephalitis (Huizinga and McLaughlin <xref ref-type="bibr" rid="CR83">1990</xref>
; Sykora et al. <xref ref-type="bibr" rid="CR180">1983</xref>
). In the USA, the emergence of most water-borne outbreaks was associated with severe precipitation (Rose et al. <xref ref-type="bibr" rid="CR166">2001</xref>
).</p>
<p id="Par12">The most famous water-borne disease is the cholera, a bacterial diarrheal disease caused by <italic>Vibrio cholerae</italic>
. The disease is transmitted by drinking contaminated water. Cholera is a highly temperature-dependent disease which increases with the increase in water temperature. Infection due to <italic>Vibrio</italic>
spp. is an example of the influence of global warming and ecology on the emergence of pathogens. The increase in water temperature affects the plankton population in water. The symbiotic relationship between vibrio and plankton leads to the increase in abundance of vibrio population. Swimmers who have open wounds and shellfish consumers can easily attract the infection. Similarly, <italic>Vibrio cholera</italic>
is associated with zooplankton and both V. cholera and zooplankton population will bloom when the water temperature increases (Redshaw et al. <xref ref-type="bibr" rid="CR160">2013</xref>
). The prevalence of Vibrio associated diseases increased clearly worldwide in the last decades and could even emerge in many Northern European countries as a response to global warming (Pascual et al. <xref ref-type="bibr" rid="CR148">2000</xref>
; Semenza et al. <xref ref-type="bibr" rid="CR172">2012</xref>
). The infections spread in warm summers via swimming pools and in coastal cities (Andersson and Ekdahl <xref ref-type="bibr" rid="CR5">2006</xref>
; Baker-Austin et al. <xref ref-type="bibr" rid="CR12">2013</xref>
; Frank et al. <xref ref-type="bibr" rid="CR58">2006</xref>
; Schets et al. <xref ref-type="bibr" rid="CR169">2006</xref>
). The spread of water-borne epidemics as leptospirosis and gastrointestinal infections is usually associated with heavy rainfall and floods (Cann et al. <xref ref-type="bibr" rid="CR29">2013</xref>
).</p>
<p id="Par13">The increase in temperature will selectively adapt fungi to higher environmental temperatures which resample that of mammals. So that pathogenic fungi, which are at the time not pathogenic for mammals due to their body temperature, will be capable of infecting mammals in the future (Garcia-Solache and Casadevall <xref ref-type="bibr" rid="CR62">2010</xref>
). Climatic factors can also promote the spread of non-infectious diseases (e.g. the increase in humidity, temperature and rainfalls enhance the growth of fungi and the spread of mycotoxin related diseases). In warm summer, many factors interact leading to the increase in cases of food poisoning such as enhanced bacterial survival, the people spend more time outside where they eat and drink, and finally due to the increase in the insect/rodent population and activity (El-Sayed et al. <xref ref-type="bibr" rid="CR53">2008</xref>
; Milazzo et al. <xref ref-type="bibr" rid="CR121">2017</xref>
; Park et al. <xref ref-type="bibr" rid="CR144">2018</xref>
; Touchon et al. <xref ref-type="bibr" rid="CR189">2009</xref>
).</p>
</sec>
<sec id="Sec4"><title>Insects and insect-borne diseases</title>
<p id="Par14">Global warming influences both vector host dimensions in a way which controls their spatiotemporal expansion and the emergence of the diseases in a complex but balanced way (Morgan et al. <xref ref-type="bibr" rid="CR129">2001</xref>
; Renn et al. <xref ref-type="bibr" rid="CR161">2011</xref>
). Vector-borne pathogens are usually geographically restricted to certain areas where their vectors exist. However, the emergence of the transmitting vectors to new districts as a result of global warming is logically associated with the emergence of these vector-borne pathogens (Cann et al. <xref ref-type="bibr" rid="CR29">2013</xref>
). In the last years, several diseases could emerge in Europe in relation to their vector expansion such as dengue fever, West Nile fever, chikungunya fever, malaria, leishmaniasis, Lyme disease and tick-borne encephalitis (Baylis <xref ref-type="bibr" rid="CR14">2017</xref>
).</p>
<p id="Par15">The emerging of new infectious diseases due to the geographical expansion of the insect vector should not be underestimated. One vector (e.g. <italic>Aedes albopictus</italic>
) can alone transmit at least 22 different types of arboviruses in addition to various parasitic diseases such as dengue fever, yellow fever, West Nile virus, Eastern equine encephalitis, chikungunya virus, Ross River virus, Usutu virus, and the nematodes <italic>Dirofilaria immitis</italic>
and <italic>D. repens</italic>
(Redshaw et al. <xref ref-type="bibr" rid="CR160">2013</xref>
).</p>
<p id="Par16">The northern expansion of vectors like ticks and mosquitoes lead to the emergence of VBDs in North America and Scandinavian. The tick-borne diseases include diseases like babesiosis, anaplasmoses, and Powassan encephalitis, while the mosquito-borne diseases involve diseases like dengue fever and malaria. Other victors like sandflies introduced diseases like Lyme disease, Boutonneuse fever and leishmaniasis. Similarly, the southern expansion of victors in Australia increased the prevalence of insect-borne diseases according to health records such as Ross River virus, Murray Valley encephalitis and Barmah Forest virus (Greer et al. <xref ref-type="bibr" rid="CR70">2008</xref>
).</p>
</sec>
<sec id="Sec5"><title>Mosquito</title>
<p id="Par17">While the increase in temperature enables the survival of mosquitoes and the elongation of their season of activity, heavy rainfalls are also necessary to provide standing water surface required for egg-laying and larval development. High levels of air humidity enhance the vector population dynamics. Finally, the wind plays an important role in the spread of mosquitoes and their associated diseases. The wind was incriminated to be the reason for the emergence of <italic>Culex tritaeniorhynchus</italic>
mosquitoes in several areas in China (Min and Xue <xref ref-type="bibr" rid="CR122">1996</xref>
; Walsh et al. <xref ref-type="bibr" rid="CR193">2008</xref>
).</p>
<p id="Par18">Three genera of mosquitoes (<italic>Aedes</italic>
, <italic>Culex</italic>
and <italic>Anopheles</italic>
) are the mostly incriminated in transmission of diseases to men and animals. The mosquito-borne diseases may expand either through the emergence of the victor species to a new area or through the adaptation of the introduced mosquito-borne pathogen to native mosquito species which already exist in this location. The best example for that is the chikungunya virus which is usually transmitted by <italic>Aedes albopictus</italic>
. Following its emergence in Europe, the native European mosquito species such as <italic>Ae. geniculate</italic>
were found to be highly susceptible to chikungunya virus infection and can replace <italic>Aedes albopictus</italic>
in disease epidemiology (Ng et al. <xref ref-type="bibr" rid="CR133">2019</xref>
; Prudhomme et al. <xref ref-type="bibr" rid="CR155">2019</xref>
). The best example for the second possibility is seen by <italic>Aedes aegypti</italic>
which is endemic in Africa. The exotic mosquito species emerged in the Netherlands but could not persist due to the unsuitable environmental conditions. In opposite to the case in Portugal where the invader species could establish itself in 2002 and induced dengue fever outbreak a few years later in 2012 (Scholte et al. <xref ref-type="bibr" rid="CR171">2010</xref>
; Sousa et al. <xref ref-type="bibr" rid="CR177">2012</xref>
). Similarly, invasive <italic>Aedes</italic>
species could be routinely detected between the years 2016 and 2018 in different localities in Canada (June <xref ref-type="bibr" rid="CR91">2018</xref>
).</p>
<p id="Par19">However, beside the effects of environmental changes which favour the increase in insect population, human activities may also induce changes in mosquito population as was seen in Belgium. The intensive rearing of pigs and the collection of manure nearby enabled the shift in larval habitat from tree holes in forests to the pig farm manure (Dekoninck et al. <xref ref-type="bibr" rid="CR42">2011</xref>
). At the time, at least 8 human pathogenic insect-borne viruses from the families are circulating in European populations, namely, sindbis and chikungunya (Togaviridae), Batai, Tayna, snowshoe hare and Inkoo (Bunyaviridae) and finally West Nile, Usutu, and dengue (Flaviviridae) (Vazquez et al. <xref ref-type="bibr" rid="CR192">2011</xref>
).</p>
<p id="Par20">When we investigate the mosquito-borne diseases such as dengue fever, yellow fever, and chikungunya virus (transmitted by Aedes species), West Nile fever, Eastern equine encephalitis and heartworm infection (by several mosquito species including <italic>Anopheles</italic>
, <italic>Aedes</italic>
, <italic>Culex</italic>
, <italic>Culiseta</italic>
, <italic>Coquillettidia</italic>
, <italic>Deinocerites</italic>
, <italic>Mansonia</italic>
, <italic>Orthopodomyia</italic>
, <italic>Psorophora</italic>
and <italic>Uranotaenia</italic>
), Ross River fever and Usutu virus infection (by Culex and Aedes) and malaria (by <italic>Anopheles</italic>
and <italic>Aedes</italic>
) (Redshaw et al. <xref ref-type="bibr" rid="CR160">2013</xref>
), we would notice that one mosquito species (<italic>Aedes aegypti</italic>
) out of 3500 mosquito species is responsible for most serious outbreaks and can transmit most of the mosquito-borne pathogens outside Africa (Powell <xref ref-type="bibr" rid="CR154">2018</xref>
). While <italic>Aedes aegypti</italic>
is common in Africa, another species which originates from Asia (tiger mosquito <italic>Aedes albopictus</italic>
) emerged in Europe and North America and was considered as the most invasive mosquito species and one of top 100 invasive insect species worldwide. Tiger mosquitoes are known for being very aggressive diurnal-biting insects. It can transmit more than 20 pathogens to humans alone (Ogden et al. <xref ref-type="bibr" rid="CR137">2014</xref>
). Tiger mosquitoes are responsible for the emergence of several diseases to Europe such as chikungunya fever (Italy in 2007 and France in 2010) (Fischer et al. <xref ref-type="bibr" rid="CR56">2013</xref>
). The emergence and expansion of <italic>A. albopictus</italic>
in the Western Hemisphere enhanced the emergence and endemicity of <italic>A. albopictus-</italic>
borne diseases like chikungunya virus infection and dengue fever in Italy, France and Croatia in Europe, and in Hawaii, Texas and Florida in USA. West Nile virus became now also endemic in North America after its emergence due to migratory birds (Redshaw et al. <xref ref-type="bibr" rid="CR160">2013</xref>
).</p>
<p id="Par21">According to the published data, three major emerging mosquito-borne viruses represent a global challenge for public health: (1) West Nile virus (WNV), an insect-borne virus which induces fatal encephalitis in mammals, humans and even birds. The virus is transmitted by <italic>Culex</italic>
mosquitoes. Like other mosquito-borne diseases, the disease expanded its geographic range to emerge in new countries as a result of climatic changes. The disease emerged in South America in 2003 and induced a large outbreak in Europe in 2010 (involved Greece, Romania, Hungary, Spain, Russia, Turkey and Italy) (Paz <xref ref-type="bibr" rid="CR149">2015</xref>
). The disease was also detected in other European countries such as France, Portugal and Serbia. The source of the invading viruses was confirmed to be from Israel, Morocco and Turkey. Later on, in 2018, the virus emerged for the first time in Germany (Ziegler et al. <xref ref-type="bibr" rid="CR196">2019</xref>
). In 1999, WNV first emerged in New York (USA), the increase in mosquito population due to the increase rainfalls and the lengthening of the mosquito activity season due to the increase in temperature leads to the increase of the prevalence of the disease. In 2013, 2170 cases of WNF were reported in USA with 88 fatalities (Kilpatrick et al. <xref ref-type="bibr" rid="CR96">2006</xref>
; Paz <xref ref-type="bibr" rid="CR149">2015</xref>
). (2) Chikungunya virus is transmitted by <italic>Aedes</italic>
mosquitoes. In the last decade, <italic>Ae. Albopictus</italic>
spread in Europe, North and South America, and many countries in Africa; this resulted in the recent emergence of the chikungunya virus to more than 40 countries worldwide (Sanyaolu et al. <xref ref-type="bibr" rid="CR168">2016</xref>
). The increase in temperature was found to be linearly related to the increase in disease prevalence (Dhimal et al. <xref ref-type="bibr" rid="CR46">2015b</xref>
). The epidemiological map of the diseases indicated its confirmed existence in at least in 98 countries (24 in Africa, 20 in Asia, 44 in North and South America, 10 countries in Pacific Islands) (Sanyaolu et al. <xref ref-type="bibr" rid="CR168">2016</xref>
). Additionally, the virus emerged in 2007 for the first time in Europe (Italy) where it infected at least 200 persons (Rezza et al. <xref ref-type="bibr" rid="CR163">2007</xref>
). Later on, in 2010, the highly aggressive Asian tiger mosquito (<italic>Ae. Albopictus</italic>
) spread both chikungunya and dengue viruses to France and Croatia, and in 2012 to Portugal (Sousa et al. <xref ref-type="bibr" rid="CR177">2012</xref>
). However, a part of this ability to widespread is attributed to its genetic mutation which enabled the virus to use Asian tiger mosquito as a vector and not being restricted to yellow fever mosquito alone (CE TKVDM <xref ref-type="bibr" rid="CR33">2007</xref>
). (3) Zika virus which induced serious public health problems in South America between 2015 and 2016 is expected to emerge in Europe as both of its vectors <italic>Ae. aegypti</italic>
and <italic>Ae. albopictus</italic>
are endemic in Europe (Caminade et al. <xref ref-type="bibr" rid="CR28">2017</xref>
).</p>
<p id="Par22">Other mosquito-borne viruses are also investigated. Repeated horse outbreaks with the mosquito-borne Eastern equine encephalitis virus could be detected in Ontario in 2008, 2009 and 2010. The virus reported its first human infection in 2016 (Chénier et al. <xref ref-type="bibr" rid="CR35">2010</xref>
; Ludwig et al. <xref ref-type="bibr" rid="CR107">2019</xref>
). Other mosquito-borne viruses include the following: (1) Usutu virus (flavivirus) was isolated for the first time from human patients in Italy in 2009 and from migrating birds in Germany in 2011 (Vazquez et al. <xref ref-type="bibr" rid="CR192">2011</xref>
). At the time, the viruses seem to be circulating in several European countries (Gaibani and Rossini <xref ref-type="bibr" rid="CR60">2017</xref>
). (2) Rift Valley fever virus (Bunyaviridae: Phlebovirus) is a serious emerging zoonotic disease in Africa and the Middle East. The disease has a great economic impact and represents a public health concern. Like other emerging insect-borne diseases, the global warming supports their geographical expansion. The virus was introduced to Europe in 2016 through a French service member in Mali who caught the infection in Mali before travelling to France via Crete, Greece. Fortunately, the disease did not persist there (Tong et al. <xref ref-type="bibr" rid="CR188">2019</xref>
). (3) Yellow fever is a tropical viral disease which started to induce outbreaks in South America (in particular in Brazil and Argentina). Although North America and Europe are free of the virus, the virus emerged in both continents in the past (seventeenth and nineteenth centuries) according to WHO. In the last decades, the virus started to invade new countries in association with mosquito active seasons (Report W <xref ref-type="bibr" rid="CR162">2015</xref>
), and finally, the bluetongue virus emerged in 2006–2007 across 12 European countries in northern Europe and UK. The wind is believed to be responsible for the disease introduction to Europe by spreading the vector (<italic>Cu. imicola</italic>
) northward. Beside the main vector (<italic>Cu. imicola</italic>
), additional native European species (<italic>Cu. obsoletus</italic>
, <italic>Cu. pulicaris</italic>
, <italic>Cu. chiopterus</italic>
and <italic>Cu. dewulfi</italic>
) shared in the spread of the virus across Europe (Gould and Higgs <xref ref-type="bibr" rid="CR68">2009</xref>
; Molyneux <xref ref-type="bibr" rid="CR124">2009</xref>
; Purse et al. <xref ref-type="bibr" rid="CR156">2005</xref>
) (Table <xref rid="Tab2" ref-type="table">2</xref>
).<table-wrap id="Tab2"><label>Table 2</label>
<caption><p>Some common examples of emerging and re-emerging diseases infecting human, animals or both</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th></th>
<th>Bacterial diseases</th>
<th>Viral diseases</th>
<th>Parasitic diseases</th>
</tr>
</thead>
<tbody><tr><td>Human</td>
<td><p>• Tuberculosis</p>
<p>• Hemorrhagic colitis (HC) and haemolytic uremic syndrome (HUS) caused by <italic>Shiga</italic>
Toxin producing <italic>E. coli</italic>
(STEC)</p>
</td>
<td><p>• Coronavirus disease 19 (COVID-19)</p>
<p>• Middle East respiratory syndrome coronavirus (MERS)</p>
<p>• Severe acute respiratory syndrome coronavirus (SARS)</p>
<p>• Ebola virus infection</p>
</td>
<td><p>• Malaria</p>
<p>• Schistosomiasis</p>
</td>
</tr>
<tr><td>Animal</td>
<td><p>• Swine edema (by Stx2e producing <italic>E. coli</italic>
)</p>
<p>• <italic>Bartonella henselae</italic>
</p>
<p>• <italic>Pasteurella multocida infections</italic>
</p>
</td>
<td>• Swine acute diarrhoea syndrome coronavirus (SADS-CoV)</td>
<td><p>• Fasciola</p>
<p>• Trypanosomiasis</p>
</td>
</tr>
<tr><td>Zoonotic</td>
<td><p>• Methicillin-resistant <italic>Staphylococcus aureus</italic>
(MERSA)</p>
<p>• Leptospirosis</p>
</td>
<td><p>• West Nile fever</p>
<p>• Rabies</p>
<p>• Avian influenza</p>
</td>
<td><p>• Leishmaniasis</p>
<p>• Ascariasis</p>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
<p id="Par23">Mosquito is also capable of transmitting parasitic diseases such as malaria and filariasis. Malaria is the most serious and fatal parasitic disease worldwide with more than 214 million annual clinical cases and half a million deaths, 90% of which live in Africa. These numbers are expected to expand in response to global warming. The situation is additionally complicated due to the growing resistance against anti-plasmodium drugs and by mosquitoes against insecticides (Gunda et al. <xref ref-type="bibr" rid="CR71">2017</xref>
; Ssempiira et al. <xref ref-type="bibr" rid="CR178">2018</xref>
). Historically, malaria invaded Europe on many occasions. Old reports from ancient Roma reported the presence of Malaria in Italy thousands of years ago (Micallef <xref ref-type="bibr" rid="CR120">2016</xref>
; Sallares <xref ref-type="bibr" rid="CR167">2002</xref>
). Newer reports from the year 1265 reported the presence of malaria in Croatia; seventeenth century documented the re-introduction of malaria to Europe through Spain. However, in the twentieth century, WHO launched a global malaria eradication program which resulted in the eradication of malaria from 79 countries worldwide (mainly in Eurasia, Australia, northern America, and northern Africa with the exception of Turkey and countries of middle Asia including Azerbaijan, Georgia, Kyrgyzstan and Tajikistan) (Askling et al. <xref ref-type="bibr" rid="CR10">2012</xref>
; Caminade et al. <xref ref-type="bibr" rid="CR27">2014</xref>
). The eradication of malaria from Europe was officially declared in 1975 and was achieved via the drainage of wetland and stagnant water, chemical treatment of patients, biological control of the mosquito larvae using the fish <italic>Gambusia holbrooki</italic>
, improvement of water system and sewage infrastructure (Talapko et al. <xref ref-type="bibr" rid="CR181">2019</xref>
). However, recently, between 2009 and 2012, several cases were diagnosed in Greece (Danis et al. <xref ref-type="bibr" rid="CR39">2011</xref>
). Later on, malaria was re-introduced in Croatia, Italy, Malta, Bulgaria, France, Germany and Spain (Krüger et al. <xref ref-type="bibr" rid="CR99">2001</xref>
; Medialdea-Carrera et al. <xref ref-type="bibr" rid="CR117">2018</xref>
; Monge-Maillo and López-Vélez <xref ref-type="bibr" rid="CR125">2012</xref>
). In Greece, in 2011, <italic>Plasmodium vivax</italic>
could be isolated from the blood of 40 patients from different regions of the country. The patients were infected locally as they have no travelling history to the outside (Ivanescu et al. <xref ref-type="bibr" rid="CR86">2016</xref>
). In the same year, in Romania, malaria was also diagnosed but fortunately, the disease was imported with travellers from Italy (Neghina et al. <xref ref-type="bibr" rid="CR132">2011</xref>
; Nicolescu et al. <xref ref-type="bibr" rid="CR134">2016</xref>
). However, and although most countries in Europe are malaria-free since decades, the <italic>Anopheles</italic>
vector continued to live and exist there. The persistence of the vector represents a great threat for the re-emerge of the diseases any time, and it is expected to re-emerge in the rest of Europe and USA as the climatic changes favour the re-emergence of the disease (Askling et al. <xref ref-type="bibr" rid="CR10">2012</xref>
). These speculations are supported by computer modelling programs which predict the re-emergence of malaria in Europe and USA in the near future (Kuhn et al. <xref ref-type="bibr" rid="CR100">2003</xref>
). On the other hand, in the already endemic countries such as Iran and Zimbabwe, the prevalence of malaria increased in the last few years as reported (Babaie et al. <xref ref-type="bibr" rid="CR11">2018</xref>
; Gunda et al. <xref ref-type="bibr" rid="CR71">2017</xref>
).</p>
<p id="Par24">The development of malaria inducing <italic>Plasmodium vivax</italic>
and <italic>P. falciparum</italic>
is highly influenced by environmental temperature. The global warming is expected to result in a 12–27% increase in disease prevalence and therefore threaten the life of an additional 200 million persons (Redshaw et al. <xref ref-type="bibr" rid="CR160">2013</xref>
).</p>
</sec>
<sec id="Sec6"><title>Tick-borne diseases</title>
<p id="Par25">The association between global warming and the emergence of tick-borne diseases is well documented in Europe and Euroasia (Andreassen et al. <xref ref-type="bibr" rid="CR6">2012</xref>
; Daniel et al. <xref ref-type="bibr" rid="CR38">2003</xref>
; Gilbert <xref ref-type="bibr" rid="CR66">2010</xref>
; Jore et al. <xref ref-type="bibr" rid="CR90">2011</xref>
; Lindgren <xref ref-type="bibr" rid="CR104">2000</xref>
; Tokarevich et al. <xref ref-type="bibr" rid="CR185">2011</xref>
). These data were also confirmed by long-term studies over 30 years of tick expansion observation in Sweden (Jaenson et al. <xref ref-type="bibr" rid="CR88">2012</xref>
). Like mosquitoes, several tick species expanded their habitat to higher elevations and toward the north in Canada and Europe due to global warming which elongated the season of tick activity and enhanced their survival in the environment. This, in turn, was also reflected on the spread of tick-borne diseases such as Anaplasmosis, Babesiosis Powassan viruses and <italic>Rickettsia Helvetica</italic>
, <italic>Neoehrlichia mikurensis</italic>
and <italic>Borrelia miyamotoi</italic>
diseases (Bouchard et al. <xref ref-type="bibr" rid="CR25">2019</xref>
; Jado et al. <xref ref-type="bibr" rid="CR87">2007</xref>
; Kawahara et al. <xref ref-type="bibr" rid="CR93">2004</xref>
).</p>
<p id="Par26">Although ticks can transmit the most diverse array of pathogens than all other arthropod vectors, fortunately, the tick-borne diseases emerge usually much slower than mosquito-borne diseases (Wikel <xref ref-type="bibr" rid="CR195">2018</xref>
). Ticks alone were found to transmit at least 95% of known insect-borne diseases in the USA (Adams et al. <xref ref-type="bibr" rid="CR1">2015</xref>
).</p>
<p id="Par27">The expansion of <italic>Ixodes ricinus</italic>
ticks (victor of <italic>Borrelia burgdorferi</italic>
spirochetes) poleward in Europe and Eurasia is well documented. The tick could be detected in UK, Germany, Sweden and Russia (Cull et al. <xref ref-type="bibr" rid="CR37">2018</xref>
; Jaenson et al. <xref ref-type="bibr" rid="CR88">2012</xref>
; Mannelli et al. <xref ref-type="bibr" rid="CR111">2012</xref>
). The expansion of another tick species in Europe and Eurasia was also reported (<italic>Dermacentor reticulatus</italic>
) which is the vector of tick-borne encephalitis virus, Omsk haemorrhagic fever virus, <italic>Rickettsia slovaca</italic>
, <italic>Rickettsia raoultii</italic>
, <italic>Anaplasma marginale</italic>
, <italic>Babesia canis</italic>
, <italic>Babesia caballi</italic>
and <italic>Theileria equi</italic>
(Altizer et al. <xref ref-type="bibr" rid="CR3">2013</xref>
; Földvári et al. <xref ref-type="bibr" rid="CR57">2016</xref>
). Similar reports documented the extension of the habitat of the tick species <italic>Ixodes scapularis</italic>
(transmit Lyme borreliosis), <italic>Amblyomma americanum</italic>
(vector of <italic>Amblyomma americanum</italic>
transmitted <italic>Ehrlichia chaffeensis</italic>
and <italic>Ehrlichia ewingii</italic>
) and <italic>Amblyomma maculatum</italic>
(transmit <italic>Rickettsia parkeri</italic>
, potted fever agent, and the canine apicomplexian (<italic>Hepatozoon americanum</italic>
)) and <italic>Hemaphysalis longicornis</italic>
to involve new land in North America (Eisen and Eisen <xref ref-type="bibr" rid="CR50">2018</xref>
; Ogden and Lindsay <xref ref-type="bibr" rid="CR136">2016</xref>
; Paddock and Goddard <xref ref-type="bibr" rid="CR142">2015</xref>
; Sonenshine <xref ref-type="bibr" rid="CR176">2018</xref>
)<italic>.</italic>
Human cases of tick-borne babesiosis were recently reported in Canada, Europe and Japan (Kulkarni et al. <xref ref-type="bibr" rid="CR101">2015</xref>
; Vannier and Krause <xref ref-type="bibr" rid="CR190">2012</xref>
, <xref ref-type="bibr" rid="CR191">2020</xref>
).</p>
<p id="Par28">Tick expansion is promoted by the warmer winters in the last decade due to global warming (Porretta et al. <xref ref-type="bibr" rid="CR152">2013</xref>
; Tokarevich et al. <xref ref-type="bibr" rid="CR185">2011</xref>
). In the last few years, more than 11 bacterial tick-borne human emerged pathogens were detected in Europe which include various Rickettsiae and Borrelia species (Parola and Raoult <xref ref-type="bibr" rid="CR145">2001</xref>
). Ticks transmitted by migrating birds also play an epidemiological role in the spread of the pathogens. In one study, 16 out of 43 migrating bird species were infested with at least one tick. The ticks were positive for <italic>C. burnetii</italic>
, <italic>Rickettsia</italic>
spp. and <italic>R. helvetica</italic>
in addition to <italic>Babesia microti</italic>
, <italic>B. capreoli</italic>
and <italic>B. venatorum</italic>
in variable degrees (Lu et al. <xref ref-type="bibr" rid="CR106">2016</xref>
). Beside the birds, the epidemiological role of ticks in the transmission of zoonotic bacteria <italic>Coxiella burnetii</italic>
was recently confirmed (Berthová et al. <xref ref-type="bibr" rid="CR18">2016</xref>
; Koehler et al. <xref ref-type="bibr" rid="CR97">2019</xref>
; Pacheco et al. <xref ref-type="bibr" rid="CR140">2013</xref>
).</p>
<p id="Par29">Recent reports listed the main tick-borne pathogens endemic in Europe, such as <italic>Rickettsia</italic>
, <italic>A. phagocytophilum</italic>
, <italic>Borrelia burgdorferi</italic>
, <italic>Babesia</italic>
spp., <italic>Borrelia miyamatoi</italic>
, <italic>Bartonella henselae</italic>
, Candidatus <italic>N. mikurensis</italic>
, <italic>Francisella tularensis</italic>
and the viruses Crimean-Congo haemorrhagic fever virus (CCHFV) and the tick-borne encephalitis (TBEV). The prevalence and their geographical distribution are expanding (Amicizia et al. <xref ref-type="bibr" rid="CR4">2013</xref>
; Hartemink and Takken <xref ref-type="bibr" rid="CR78">2016</xref>
; Jaenson et al. <xref ref-type="bibr" rid="CR88">2012</xref>
). In addition, ticks are also capable of transmitting a large number of serious zoonotic viruses. The spread of the resulting diseases is coupled with the geographical expansion of ticks and their emergence in new areas (Kazimírová et al. <xref ref-type="bibr" rid="CR94">2017</xref>
; Tokarz et al. <xref ref-type="bibr" rid="CR186">2014</xref>
, <xref ref-type="bibr" rid="CR187">2018</xref>
). The list of the transmitted viruses includes Phlebovirus (induces thrombocytopenia and high fever) (Fatmi et al. <xref ref-type="bibr" rid="CR55">2017</xref>
; Holbrook <xref ref-type="bibr" rid="CR82">2012</xref>
; McMullan et al. <xref ref-type="bibr" rid="CR116">2012</xref>
), Bourbon virus, Powassan virus, tick-borne encephalitis viruses complex, CCHFV and Alkhurma haemorrhagic fever virus (Mansfield et al. <xref ref-type="bibr" rid="CR112">2009</xref>
)<italic>.</italic>
</p>
<p id="Par30">Tick-borne encephalitis (TBE) and Lyme disease emerged in Europe in connection to tick expansion. Cases of both diseases were even reported in Scandinavia. The disease prevalence is increasing in an alarming way due to global warming and northwards emergence of tick vector (Lindgren <xref ref-type="bibr" rid="CR104">2000</xref>
; Lukan et al. <xref ref-type="bibr" rid="CR108">2010</xref>
; Randolph <xref ref-type="bibr" rid="CR158">2004</xref>
). Since the mid-1980s, the winter in Scandinavian got warmer. Since then, the prevalence of TBE increases steadily and clearly. Many factors are believed to be the actual reasons for this increase, mainly the climatic changes (Andreassen et al. <xref ref-type="bibr" rid="CR6">2012</xref>
; Lindgren and Gustafson <xref ref-type="bibr" rid="CR105">2001</xref>
). One of the TBE complex viruses is the Louping ill virus. The disease was also recently detected in Europe and UK (Gilbert <xref ref-type="bibr" rid="CR67">2016</xref>
).</p>
<p id="Par31">A second zoonotic tick-borne emerging viral diseases in Europe is the Congo haemorrhagic fever (CCHF). The CCHFV represents a great public health concern in Europe due to its high human fatality (Papa et al. <xref ref-type="bibr" rid="CR143">2015</xref>
). The virus is transmitted by Hyalomma tick to ruminants, and now it became endemic in Africa, the Middle East, the Balkan Peninsula, Eastern and South Europe and Asia. Warmer climatic conditions allow the ticks to invade and emerge in new areas (Baylis <xref ref-type="bibr" rid="CR14">2017</xref>
). Additionally, ticks are responsible for the emergence of Piroplasmorida (such as Babesia and Theileria). Babesiosis is the most important tick-borne protozoal disease to cattle industry. The disease is a global animal health problem responsible for great economic losses in the veterinary sector. The emerging zoonosis represents a great challenge of public health due to the exponential increase of babesiosis worldwide facilitated by the geographic expansion of ticks induced by global warming (Beugnet and Chalvet-Monfray <xref ref-type="bibr" rid="CR19">2013</xref>
, Florin). At the time, there are more than 100 known babesia species, half of them are recently discovered (Florin). Many of them have zoonotic importance such as <italic>B. microti</italic>
, <italic>B. microti</italic>
-like organisms, <italic>B. duncani</italic>
, <italic>B. duncani</italic>
-like organisms, <italic>B. divergens</italic>
, <italic>B. divergens</italic>
-like organisms and <italic>B. venatorum</italic>
(Vannier and Krause <xref ref-type="bibr" rid="CR191">2020</xref>
).</p>
<p id="Par32">Beside Babesia, the <italic>Anaplasma</italic>
and <italic>Ehrlichia</italic>
are also important tick-borne pathogens of zoonotic importance (Brown and Barbet <xref ref-type="bibr" rid="CR26">2016</xref>
). The tick-borne disease caused by <italic>Anaplasma phagocytophilum</italic>
is a serious zoonotic disease which infects humans, cattle, equines and canines. The disease can be transmitted by different tick species endemic in Europe (e.g. <italic>Ixodes ricinus</italic>
), North America (e.g. <italic>Ixodes scapularis</italic>
, <italic>Ixodes pacificus</italic>
and <italic>Ixodes spinipalpis</italic>
) and Asia (e.g. <italic>Ixodes persulcatus</italic>
) (Stuen et al. <xref ref-type="bibr" rid="CR179">2013</xref>
).</p>
<p id="Par33">Beside Anaplasma, the closely related tick-borne <italic>Ehrlichia</italic>
can also infect human and animals. The diseases can be induced by <italic>Ehrlichia chaffeensis</italic>
and <italic>Ehrlichia ewingii</italic>
(Monocytes Ehrlichiosis) in human or heartwater in cattle (by <italic>Ehrlichia ruminantium</italic>
) (Allsopp <xref ref-type="bibr" rid="CR2">2015</xref>
; Paddock and Childs <xref ref-type="bibr" rid="CR141">2003</xref>
; Thomas et al. <xref ref-type="bibr" rid="CR183">2009</xref>
). Other forms of ehrlichiosis can also be induced by other Ehrlichia species like <italic>Ehrlichia canis</italic>
, <italic>Ehrlichia muris</italic>
and <italic>Ehrlichia mineirensis</italic>
. As a tick-borne pathogen, Ehrlichia species could be detected almost worldwide (Allsopp <xref ref-type="bibr" rid="CR2">2015</xref>
).</p>
<p id="Par34">The northward expansion of the dog tick <italic>Rhipicephalus sanguineus</italic>
is alarming due to their role in the emergence of the life-threatening pathogens such as <italic>Rickettsia rickettsii</italic>
and <italic>R. conorii</italic>
, the causative agents of Rocky Mountain spotted fever and Mediterranean spotted fever, respectively (Parola et al. <xref ref-type="bibr" rid="CR147">2008</xref>
). The related tick-borne <italic>Rickettsia and Borrelia</italic>
species usually emerge parallel to <italic>Anaplasma and Ehrlichia</italic>
as they are also transmitted by a large variety of tick species<italic>.</italic>
The emergence of <italic>Borrelia</italic>
bacteria in addition to TBE virus resulted in huge concern in Europe (Gage et al. <xref ref-type="bibr" rid="CR59">2008</xref>
).</p>
<p id="Par35">The ticks can also transmit various bacterial diseases such as Lyme borreliosis. In the last decade, the prevalence of the disease in Europe increased not only in endemic areas but also expanded to new geographical regions, particularly in Netherlands and Belgium. It is estimated that Lyme borreliosis (bacterial spirochaete disease) infects yearly at least 85,000 people in Europe (Gassner and van Overbeek <xref ref-type="bibr" rid="CR63">2007</xref>
; Hofhuis et al. <xref ref-type="bibr" rid="CR81">2015</xref>
). The disease is caused mainly by <italic>Borrelia burgdorferi</italic>
and <italic>Borrelia mayonii</italic>
in Europe. However, other species of <italic>Borrelia</italic>
like <italic>Borrelia spielmanii</italic>
, <italic>Borrelia bavariensis</italic>
, <italic>Borrelia afzelii</italic>
and <italic>Borellia garinii</italic>
were also reported in North America and Euroasia as potent zoonotic spirochetes transmitted by <italic>Ixodes ricinus</italic>
complex (Kernif et al. <xref ref-type="bibr" rid="CR95">2016</xref>
; Merhej et al. <xref ref-type="bibr" rid="CR119">2014</xref>
; Parola et al. <xref ref-type="bibr" rid="CR146">2005</xref>
; Rizzoli et al. <xref ref-type="bibr" rid="CR165">2011</xref>
). In addition ticks, fleas and flies can aid in the expansion of rabbit fever (tularemia), a zoonotic vector-borne disease caused by <italic>Francisella tularensis</italic>
(Nakazawa et al. <xref ref-type="bibr" rid="CR130">2007</xref>
).</p>
<p id="Par36">Mosquitoes and ticks are not the only insect vectors affected by global warming. Additional parasites like fleas, triatomine bugs and bloodsucking flies such as sandfly (<italic>Phlebotomus</italic>
and <italic>Lutzomyia</italic>
spp.), <italic>Glossina</italic>
tsetse flies, horsefly (<italic>Tabanus</italic>
spp.) and deerfly (<italic>Chrysops</italic>
sp.) were also incriminated in the introduction of emerging diseases to new locations such as tularemia, <italic>Yersinia pests</italic>
, Leishmaniasis and Trypanosoma in response to climatic changes (Bern et al. <xref ref-type="bibr" rid="CR17">2007</xref>
; Hargrove <xref ref-type="bibr" rid="CR77">2004</xref>
; Nakazawa et al. <xref ref-type="bibr" rid="CR130">2007</xref>
; Redshaw et al. <xref ref-type="bibr" rid="CR160">2013</xref>
).</p>
<p id="Par37">Sandflies (<italic>Phlebotomus species</italic>
) can transmit leishmaniasis (cutaneous and visceral forms). The diseases emerged in South Europe, UK and Germany and infected humans and dogs there (Dujardin et al. <xref ref-type="bibr" rid="CR48">2008</xref>
). More than 90% of the human cases live in India, Bangladesh, Sudan, South Sudan, Ethiopia or Brazil (Mitra and Mawson <xref ref-type="bibr" rid="CR123">2017</xref>
). However, <italic>Phlebotomus</italic>
spp. were recorded in Switzerland, Germany, Austria, Spain, Portugal, France, Italy, Belgium, Greece, Malta, Cyprus, Andorra and Corsica (Aransay et al. <xref ref-type="bibr" rid="CR8">2004</xref>
; Ballart et al. <xref ref-type="bibr" rid="CR13">2012</xref>
; Dereure et al. <xref ref-type="bibr" rid="CR43">2009</xref>
; ECDC <xref ref-type="bibr" rid="CR49">2013</xref>
). The sandfly expansion reached later East European countries like Bulgaria, Croatia, Albania, Bosnia and Herzegovina, Croatia, Georgia, Hungary, Montenegro, Romania, Serbia, Macedonia, Turkey and Ukraine (ECDC <xref ref-type="bibr" rid="CR49">2013</xref>
). The detection of sandfly was associated with the expansion of the leishmaniasis mainly in dogs (Boecken et al. <xref ref-type="bibr" rid="CR23">2011</xref>
; Ready <xref ref-type="bibr" rid="CR159">2010</xref>
). This expansion was attributed to global warming (Gálvez et al. <xref ref-type="bibr" rid="CR61">2011</xref>
).</p>
<p id="Par38">African trypanosomiasis (sleeping sickness) is a protozoal disease transmitted by tsetse flies and caused by <italic>Trypanosoma brucei gambiense</italic>
and <italic>T. brucei rhodesiense.</italic>
Due to the vector expansion in relationship with the global warming, it is predicted that 30,000 people will be infected by the parasite while 70 million persons will be at risk during this century (Moore et al. <xref ref-type="bibr" rid="CR127">2012</xref>
). Another type of trypanosomiasis started to emerge from Latin America, namely Chagas disease caused by <italic>Trypanosoma cruzi</italic>
and transmitted by the bites of the bloodsucking <italic>Triatoma infestans</italic>
known as the kissing bugs or orally by the consumption of water or food contaminated with the faeces of the infected bugs. The disease expansion to Central and North America was reported. At the time, it is estimated that 300,000 US residents are infected with the disease (Shikanai-Yasuda and Carvalho <xref ref-type="bibr" rid="CR173">2012</xref>
).</p>
<p id="Par39">The flea <italic>Xenopsylla cheopis</italic>
is the vector of <italic>Yersinia pestis</italic>
, the causative agent of plague. Warmer and wetter conditions are benefiting both the flea vector and <italic>Yersinia pestis</italic>
(Nakazawa et al. <xref ref-type="bibr" rid="CR130">2007</xref>
) (Ben Ari et al. <xref ref-type="bibr" rid="CR16">2008</xref>
).</p>
</sec>
<sec id="Sec7"><title>Rodents and rodent-related diseases</title>
<p id="Par40">Rodents play an important role in the epidemiology of disease emergence/re-emergence. They are capable of transmitting a large number of zoonotic disease agents either directly such as leptospirosis, Sin Nombre virus and Hantaan virus which spread via dust contaminated with dried rodent urine (Hansen et al. <xref ref-type="bibr" rid="CR76">2015</xref>
) (Pijnacker et al. <xref ref-type="bibr" rid="CR150">2016</xref>
) or indirectly as plague (Yersinia pestis). The global warming influences the change in rodent distribution maps and their population worldwide (Moore et al. <xref ref-type="bibr" rid="CR126">2011</xref>
).</p>
<p id="Par41">In conclusion, it is necessary to make all possible efforts to stop or at least to slow down the accelerated damage of the global ecosystem due to global warming and climate changes. The disturbance in the balanced ecosystems will not only lead to the emergence of infectious diseases but also has long-term serious direct and indirect damaging effects which threaten the existence of human, animals and plants (Table <xref rid="Tab3" ref-type="table">3</xref>
).<table-wrap id="Tab3"><label>Table 3</label>
<caption><p>Influence of climatic changes on health and diseases</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th colspan="12">How climatic changes influence health and diseases:</th>
</tr>
<tr><th rowspan="2" colspan="2">Agriculture (food)</th>
<th rowspan="2" colspan="2">Water resources</th>
<th rowspan="2">Tornados and wind</th>
<th colspan="5">Increase temperature and humidity</th>
<th rowspan="2" colspan="2">Mass migration of</th>
</tr>
<tr><th colspan="2">Expansion of insect niche</th>
<th colspan="2">Rodent niche</th>
<th>Direct effects on Human health</th>
</tr>
<tr><th>Food scanty</th>
<th>Food-borne diseases</th>
<th>Water scanty</th>
<th>Rains and floods</th>
<th>Airborne diseases</th>
<th>Insect/parasites</th>
<th>Insect-borne diseases</th>
<th>Rodents</th>
<th>Rodent-borne diseases</th>
<th>Physical and psychological diseases</th>
<th>Human</th>
<th>Animals</th>
</tr>
</thead>
<tbody><tr><td><p>- Diseases caused by consumption of rotted food</p>
<p>- Nutritional deficiency diseases</p>
</td>
<td><p>- Bacteria (e.g. salmonellosis)</p>
<p>- Viral (e.g. hepatitis A)</p>
</td>
<td><p>- Diseases due to consumption of contaminated water (e.g. cholera, hepatitis A, giardiasis and cryptosporidiosis)</p>
<p>- Dehydration and famines</p>
</td>
<td><p>- Fungal diseases and mycotoxins</p>
<p>- Water-borne diseases</p>
<p>-Spore-borne diseases (washed away via floods e.g. anthrax).</p>
<p>- Snail-borne diseases (e.g. trematodes)</p>
</td>
<td>- In human (e.g. wind pox) and animals (e.g. FMD).</td>
<td><p>- Such as</p>
<p>Mosquitoes</p>
<p>Ticks</p>
<p>Flies</p>
<p>Flea</p>
</td>
<td><p>- Including bacterial, viral and parasitic diseases as West Nile fever</p>
<p>Plague</p>
<p>Malaria and leishmaniasis</p>
</td>
<td>- The spread of rats and mice which has health and economic impacts</td>
<td><p>- Hanta disease</p>
<p>-Leptospirosis</p>
</td>
<td><p>- Physical diseases (e.g. sun struck, respirator asthma and heart diseases)</p>
<p>- Psychological diseases and stress borne diseases</p>
</td>
<td>Because of wars and famines which spread diseases in addition to its economic impacts</td>
<td>Due to water and food scanty which spread diseases to new areas</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
</sec>
</body>
<back><fn-group><fn><p><bold>Publisher’s note</bold>
</p>
<p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p>
</fn>
</fn-group>
<notes notes-type="ethics"><title>Compliance with ethical standards</title>
<notes notes-type="COI-statement"><title>Conflict of interest</title>
<p id="Par42">The authors declare that they have no conflict of interest.</p>
</notes>
</notes>
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